Canonical Allele Identifier: CA2063070573

Gene: MYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110913224_110913225delinsCT , CM000674.2:g.110913224_110913225delinsCT	GRCh38
NC_000012.11:g.111351028_111351029delinsCT , CM000674.1:g.111351028_111351029delinsCT	GRCh37
NC_000012.10:g.109835411_109835412delinsCT	NCBI36
NG_007554.1:g.12353_12354delinsAG , LRG_393:g.12353_12354delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228841.15:c.353+21_353+22delinsAG MANE Select	ENSP00000228841.8:n.353+21_353+22delinsAG
ENST00000663220.1:c.296+21_296+22delinsAG	ENSP00000499568.1:n.296+21_296+22delinsAG
ENST00000228841.12:c.353+21_353+22delinsAG	ENSP00000228841.7:n.353+21_353+22delinsAG
ENST00000548438.1:c.311+21_311+22delinsAG	ENSP00000447154.1:n.311+21_311+22delinsAG
ENST00000549029.1:n.205_206delinsAG
NM_000432.3:c.353+21_353+22delinsAG , LRG_393t1:c.353+21_353+22delinsAG	NP_000423.2:n.353+21_353+22delinsAG
NM_000432.4:c.353+21_353+22delinsAG MANE Select	NP_000423.2:n.353+21_353+22delinsAG